双侧肉芽肿性虹膜睫状体炎与早发性幼年银屑病关节炎相关。

IF 0.7 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmological Medicine Pub Date : 2022-10-07 eCollection Date: 2022-01-01 DOI:10.1155/2022/3990406
Christian Nieves-Ríos, Guillermo A Requejo Figueroa, Sofía C Ayala Rodríguez, Alejandra Santiago-Díaz, Eduardo J Rodriguez-Garcia, Alejandro L Perez, Erick Rivera-Grana, Adriana C Figueroa-Díaz, Rafael Martín-García, Armando L Oliver
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引用次数: 0

摘要

目的:本研究的目的是报告一例早发性幼年银屑病关节炎(JPsA)患者的双侧肉芽肿性虹膜睫状体炎。方法:采用观察性病例报告法。观察。一名三岁的西班牙女孩被送到我们的葡萄膜炎服务处进一步评估她的肉芽肿性葡萄膜炎。最初的眼科检查显示双侧角膜带病变,大量羊脂角沉淀,多发后粘连,前房细胞4+。体格检查发现左膝水肿和右腋窝皮疹。实验室检测显示红细胞沉降率为80 mm/h,抗核抗体阳性(1:1 280),人白细胞抗原B27阴性。皮肤活检证实了银屑病皮疹的诊断。口服强的松龙和外用醋酸强的松龙加硫酸阿托品治疗可使葡萄膜炎完全消退。结论和重要性。双侧肉芽肿性虹膜睫状体炎可能是早发性JPsA患者眼部受累的罕见表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bilateral Granulomatous Iridocyclitis Associated with Early-Onset Juvenile Psoriatic Arthritis.

Bilateral Granulomatous Iridocyclitis Associated with Early-Onset Juvenile Psoriatic Arthritis.

Bilateral Granulomatous Iridocyclitis Associated with Early-Onset Juvenile Psoriatic Arthritis.

Purpose: The purpose of this study is to report on a case of bilateral granulomatous iridocyclitis in a patient with early-onset juvenile psoriatic arthritis (JPsA).

Methods: The method used is an observational case report. Observations. A 3-year-old Hispanic girl was sent to our uveitis service for further evaluation of her granulomatous uveitis. The initial ophthalmologic examination revealed bilateral band keratopathy, large mutton-fat keratic precipitates, multiple posterior synechiae, and 4+ anterior chamber cells. The physical exam was notable for left knee edema and right axillary rash. Laboratory testing was remarkable for an erythrocyte sedimentation rate of 80 mm/h, positive antinuclear antibodies (1 : 1, 280), and negative human leukocyte antigen B27. A cutaneous biopsy was obtained, which confirmed the diagnosis of a psoriatic rash. Treatment with oral prednisolone and topical prednisolone acetate with atropine sulfate resulted in the complete resolution of the uveitis. Conclusion and Importance. Bilateral granulomatous iridocyclitis may be a rare presentation of ocular involvement in patients with early-onset JPsA.

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